Narita S, Asakura K, Kataura A
Department of Otolaryngology, Sapporo Medical University, Japan.
Int Arch Allergy Immunol. 1996 Feb;109(2):161-6. doi: 10.1159/000237215.
To define the role of thromboxane A2 (TxA2) in allergic rhinitis, we examined the effects of the TxA2 receptor antagonist Bay u 3405 (1, 3 and 10 mg/kg, orally) on nasal symptoms, changes in total airway resistance (TAR), histamine hypersensitivity and eosinophil infiltration into the nasal mucosa induced by topical antigen challenge in actively sensitized guinea pigs. Nasal symptoms (number of sneezes and scratches) were significantly inhibited by pretreatment with Bay u 3405, in a dose-dependent manner. We noted a biphasic increase in TAR after antigen challenge. The first peak response of TAR (177.5 +/- 6.1%, mean +/- SE) was partially but significantly inhibited by Bay u 3405 at 10 mg/kg (142.8 +/- 4.3%, p < 0.01). The second peak response of TAR (181.0 +/- 13.4%) was also inhibited by Bay u 3405 at 3 mg/kg (120.3 +/- 3.1%) and 10 mg/kg (125.2 +/- 9.4%) (both, p < 0.01). The histamine hypersensitivity induced by antigen was inhibited by Bay u 3405 at 15 mg/kg (p < 0.05). Moreover, the mean eosinophil infiltration into the nasal mucosa induced by antigen (644.1 +/- 202.6/both sides of the nasal septum) was inhibited to 137.8 +/- 69.0 by Bay u 3405 at 10 mg/kg (p < 0.05). In conclusion, our results suggest that TxA2 may play an important role in allergic rhinitis in guinea pig models.
为了明确血栓素A2(TxA2)在变应性鼻炎中的作用,我们研究了TxA2受体拮抗剂Bay u 3405(1、3和10mg/kg,口服)对主动致敏豚鼠经局部抗原激发后鼻症状、总气道阻力(TAR)变化、组胺超敏反应以及嗜酸性粒细胞浸润至鼻黏膜的影响。Bay u 3405预处理能以剂量依赖方式显著抑制鼻症状(喷嚏和搔抓次数)。抗原激发后我们观察到TAR呈双相性增加。TAR的第一个峰值反应(177.5±6.1%,平均值±标准误)在给予10mg/kg Bay u 3405时受到部分但显著的抑制(142.8±4.3%,p<0.01)。TAR的第二个峰值反应(181.0±13.4%)在给予3mg/kg(120.3±3.1%)和10mg/kg(125.2±9.4%)Bay u 3405时也受到抑制(两者均p<0.01)。抗原诱导的组胺超敏反应在给予15mg/kg Bay u 3405时受到抑制(p<0.05)。此外,抗原诱导的嗜酸性粒细胞浸润至鼻黏膜的平均值(鼻中隔两侧644.1±202.6)在给予10mg/kg Bay u 3405时被抑制至137.8±69.0(p<0.05)。总之,我们的结果提示TxA在豚鼠变应性鼻炎模型中可能起重要作用。